Benzoylhydrazine → HCID 59589853, compound
Reaction equation
P(Cl)(Cl)(Cl)=O.[N:6]1([CH2:11][CH2:12][O:13][C:14]2[CH:19]=[CH:18][C:17]([NH:20][C:21]3[N:38]=[C:24]4[CH:25]=[CH:26][CH:27]=[C:28]([C:29]5[CH:30]=[C:31]([CH:35]=[CH:36][CH:37]=5)[C:32](O)=[O:33])[N:23]4[N:22]=3)=[CH:16][CH:15]=2)[CH2:10][CH2:9][CH2:8][CH2:7]1.[C:39]([NH:47][NH2:48])(=O)[C:40]1[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=1.C(=O)([O-])O.[Na+]>>[C:40]1([C:39]2[O:33][C:32]([C:31]3[CH:30]=[C:29]([C:28]4[N:23]5[N:22]=[C:21]([NH:20][C:17]6[CH:16]=[CH:15][C:14]([O:13][CH2:12][CH2:11][N:6]7[CH2:10][CH2:9][CH2:8][CH2:7]7)=[CH:19][CH:18]=6)[N:38]=[C:24]5[CH:25]=[CH:26][CH:27]=4)[CH:37]=[CH:36][CH:35]=3)=[N:48][N:47]=2)[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=1Participants
5
Procedure
Phosphorus oxychloride (5 ml) was added dropwise to 3-{2-[4-(2-pyrrolidin-1-yl-ethoxy)-phenylamino]-[1,2,4]triazolo[1,5-a]pyridin-5-yl}-benzoic acid (50 mg, 0.113 mmol) and benzhydrazide (15 mg, 0.113 mmol). The solution was heated to reflux overnight. Once cooled the reaction mixture was added gradually to ice/water. The solution was basified with saturated aqueous sodium hydrogencarbonate and subsequently extracted twice with dichloromethane. The organics were combined, washed several times with brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The product was purified by preparatory HPLC. LCMS RT: 2.80 min, MI: 544, Method: 2.
Workup
- temperatureThe solution was heated
- temperatureto reflux overnight
- temperatureOnce cooled the reaction mixture
- extractionsubsequently extracted twice with dichloromethane
- washwashed several times with brine
- dry with materialdried over anhydrous magnesium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe product was purified by preparatory HPLC
Sources & evidence
- ORD record
- ord-8c86e037fc2f43ae83db82dfc8949a61
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09012633B2
Reaction notes
Loading…